Product Recalls in Arkansas

Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,635 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,635 in last 12 months

Showing 60416060 of 28,355 recalls

Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: RUSCHELIT Safety Clear Tracheal Tube Recalled by TELEFLEX LLC Due to Reports...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal Magill Recalled by TELEFLEX LLC Due to Reports...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Recalled by...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Magill Recalled by TELEFLEX...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Magill Recalled by TELEFLEX...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Recalled by...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal Magill Recalled by TELEFLEX LLC Due to Reports...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal Murphy Eye Recalled by TELEFLEX LLC Due to...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Recalled by...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal Murphy Eye Recalled by TELEFLEX LLC Due to...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing